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VitreQ
Vitreq B.V. · Model LF23.D03 · UDI-DI 08719214222147
MPA
Prescription
10
510(k) clearances
270
Adverse events
1
Recalls
30
Facilities
Description
23G 45° Shielded Light Fibers
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-08-05 | Alcon Research LLC | Due to incomplete seals in the pouch which provide the sterile barrier. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.